Canonical Allele Identifier: PA2741813777
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2861672
ClinVar RCV Id: RCV003605080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Asn697His
CA394486050
NM_000243.3:c.2089A>C